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Job Description Job Title: Senior Associate Scientist Immunology & Inflammation Location: Tarrytown, NY Type: Contract Compensation: Up to $55.00 Work Model: Onsite – onsite Hours: 8 AM- 5 PM M-F Responsibilities • Perform tumor implantation in mice, tumor growth measurement, injections through various routes, general surgical techniques, and collection of blood and tissue samples, • Process tissues and purify immune cells, develop and perform in vitro cell-based bioassays (primary mouse and human cells), • Investigate components of the tumor microenvironment using multi-parameter flow cytometry, • Independently design, plan, and execute experiments, and maintain accurate electronic records, • Analyze, interpret, and communicate results during internal and external meetings, • Collaborate proactively with team members to coordinate complex in vivo experiments and support cross-functional efforts Requirements • A BS or MS degree with 5+ years of experience in immuno-oncology lab research, • Hands-on experience with handling mice, tumor models, tissue processing, flow cytometry, and cell-based bioassays, • Proficient in computer skills including Microsoft Office Excel, GraphPad Prism, and FlowJo/OMIQ, • Experience designing and executing experiments, analyzing data, interpreting results, and presenting findings in an impactful manner System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. #M3 Ref: #558-Scientific

Job DescriptionJob Title: Associate Scientist Immunology & Inflammation Location: Tarrytown, NY Type: Contract Compensation: $40.00 - $45.00 per hour Contractor Work Model: Onsite Hours: 8 AM - 5 PM Responsibilities • Support respiratory and inflammatory disease research by executing in vivo experiments using mouse lung inflammation models and allorejection models, • Design, plan, and perform in vivo and in vitro assays, including tissue culture, cell-based assays, ELISA, multiplex assays (MSD/Luminex), and flow cytometry, • Process organs for immune cell isolation and analysis, • Maintain, expand, and modulate cells, evaluating results with biological and statistical software, • Analyze data using tools such as FlowJo, Omiq, Microsoft Office, MacOS, and GraphPad Prism, • Collaborate closely with cross-functional teams across the organization, • Document experimental procedures and results accurately Requirements, • BS/MS Degree in Immunology or related field; immunology experience is a plus but open to others, • Minimum of 3 years of industry experience in a relevant role, • Training in handling and care of mice, blood, and tissue sample collection and processing (strongly preferred), • Proficiency in tissue culture, cell-based assays, ELISA, multiplex assays, and flow cytometry, • Ability to independently plan and execute assays, • Experience with FlowJo, Omiq, Microsoft Office, MacOS, and GraphPad Prism, • Enthusiastic, driven, positive attitude, and effective communicator, • Ability to work in an innovative, team-driven environment System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. Ref: #558-Scientific

We're looking for experienced machine learning researchers with hands-on experience training and improving deep learning models end-to-end, across vision and language.You'll work on well-scoped empirical open-ended ML research problems.Responsibilities - Train image classifiers and generative image

What You'll Do** - Access primary sources (papers, patents) to verify protein target assignments against UniProt records - Flag and classify target assignment errors using a structured taxonomy - Propose correct UniProt accessions where assignments are wrong - Write concise, evidence-grounded notes

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Medical Director to join our Obesity team supporting our Clinical Development Unit in the area of metabolism for obesity or Type 2 diabetes. In this role, you will serve as Medical Lead for clinical trials and are responsible for the design of clinical study concepts leading to clinical trial protocols and oversight of studies, while collaborating with cross-functional stakeholders. This role requires a high-performing and highly passionate physician scientist who serves as a clinical role model for the team and demonstrates outstanding clinical scientific knowledge applicable to clinical research. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide. When & where: Location: Tarrytown, NY or Warren, NJ Travel: 10% to relevant conferences Discover your role: You guide the Global Clinical Study Team to deliver high-quality trials on time. You oversee the medical monitoring of clinical trials to ensure patient safety and adherence to regulatory guidance You lead clinical study and protocol development and present to internal and external stakeholders. You provide clinical and scientific leadership for data review, study reports, and publications. You work closely with cross-functional partners to advance program goals and key deliverables. You collaborate with discovery teams to help shape future targets and development opportunities in the field. This role requires: An M.D. or equivalent with board eligibility or board certification in Endocrinology strongly preferred; relevant experience can be acceptable. At least 2 years pharmaceutical industry experience (equivalent research in academia will be considered) Previous interactions with regulatory agencies or common technical document (CTD or "dossier") submission in an ICH region is an advantage Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Build our future together:At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Medical Director to join our Hematology team supporting Cell Therapy Clinical Development. In this role, you will provide clinical leadership and responsibility for all clinical deliverables within an assigned section of a clinical program in Hematology/Oncology, operating with minimal supervision from the Program Lead MD. Clinical deliverables may include individual protocols consistent with the Clinical Development Plan (CDP), clinical components of regulatory documents and registration dossiers, brand-related medical information, and clinical communications and publications. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a significant difference for patients worldwide.When & where:Location: Tarrytown, NY or Warren, NJTravel: 10%, to relevant congresses and conferencesDiscover your role:Manage all operational aspects and drive execution of clinical programs, in partnership with global line functions, the assigned Clinical Scientist, and Clinical Operations associates, to ensure timely execution of assigned clinical deliverables within approved budget.Lead interactions with external stakeholders (e.g., regulatory authorities, key opinion leaders, advisory boards, patient advocacy groups) and internal stakeholders (e.g., Research, Early Clinical Development, Medical Affairs, Marketing, Health Economics & Outcomes Research [HE&OR]), as well as internal decision boards.Ensure the overall safety of the compound in collaboration with the Safety Lead for the assigned programLead development of clinical sections of program-level regulatory documents, such as Investigators' Brochures, briefing books, safety updates, and IND/NDA (Investigational New Drug/New Drug Application) submission documents, and lead responses to Health Authority questionsThis role requires:A M.D. or equivalent medical degree (e.g., D.O., MBBS), preferably with clinical training in a relevant disease area such as Hematology or Oncology.Significant demonstrated experience of 4+ years in clinical research within an industry environment, spanning clinical activities across Phases 1 through 4. Cell Therapy experience preferred.Strong understanding of the global regulatory environment, including key regulatory agencies and approval processes.Strong understanding of the operational aspects of all phases of clinical trial conduct (start-up, conduct, close-out).People management experience preferred but not required.#MDJobs #MDJobsCD #GDTherapeuticJobs #Hematology #CellTherapyDoes this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit . For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.For jobs in Canada: this posting is for an existing position.Salary Range (annually)$333,300.00 - $450,900.00SummaryLocation: TARRYTOWN; WarrenType: Full time

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Medical Director to join our Hematology team supporting Cell Therapy Clinical Development. In this role, you will provide clinical leadership and responsibility for all clinical deliverables within an assigned section of a clinical program in Hematology/Oncology, operating with minimal supervision from the Program Lead MD. Clinical deliverables may include individual protocols consistent with the Clinical Development Plan (CDP), clinical components of regulatory documents and registration dossiers, brand-related medical information, and clinical communications and publications. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a significant difference for patients worldwide. Location: Tarrytown, NY or Warren, NJ Travel: 10%, to relevant congresses and conferences Manage all operational aspects and drive execution of clinical programs, in partnership with global line functions, the assigned Clinical Scientist, and Clinical Operations associates, to ensure timely execution of assigned clinical deliverables within approved budget. Lead interactions with external stakeholders (e.g., regulatory authorities, key opinion leaders, advisory boards, patient advocacy groups) and internal stakeholders (e.g., Research, Early Clinical Development, Medical Affairs, Marketing, Health Economics & Outcomes Research [HE&OR]), as well as internal decision boards. Ensure the overall safety of the compound in collaboration with the Safety Lead for the assigned program Lead development of clinical sections of program-level regulatory documents, such as Investigators' Brochures, briefing books, safety updates, and IND/NDA (Investigational New Drug/New Drug Application) submission documents, and lead responses to Health Authority questions A M.D. or equivalent medical degree (e.g., D.O., MBBS), preferably with clinical training in a relevant disease area such as Hematology or Oncology. Significant demonstrated experience of 4+ years in clinical research within an industry environment, spanning clinical activities across Phases 1 through 4. Cell Therapy experience preferred. Strong understanding of the global regulatory environment, including key regulatory agencies and approval processes. Strong understanding of the operational aspects of all phases of clinical trial conduct (start-up, conduct, close-out). People management experience preferred but not required.

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Medical Director to join our Endocrinology team supporting our Clinical Development Unit. In this role, you will serve as Medical Lead for clinical trials and are responsible for the design of clinical study concepts leading to clinical trial protocols and oversight of studies, while collaborating with cross-functional stakeholders. This role requires a high-performing and highly passionate physician scientist who serves as a clinical role model for the team and demonstrates outstanding clinical scientific knowledge applicable to clinical research. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide. Location: Tarrytown, NY, Washington, D.C., or Cambridge, MA Travel: 10% to relevant conferences Discover your role: • You guide the Global Clinical Study Team to deliver high-quality trials on time., • You oversee the medical monitoring of clinical trials to ensure patient safety and adherence to regulatory guidance, • You lead clinical study and protocol development and present to internal and external stakeholders., • You provide clinical and scientific leadership for data review, study reports, and publications., • You work closely with cross-functional partners to advance program goals and key deliverables., • You collaborate with discovery teams to help shape future targets and development opportunities in the field. This role requires: • An M.D. or equivalent with board eligibility or board certification in Endocrinology strongly preferred; relevant experience can be acceptable., • At least 2 years pharmaceutical industry experience (equivalent research in academia will be considered), • Experience in rare disease drug development strongly preferred, • Previous interactions with regulatory agencies or common technical document (CTD or "dossier") submission in an ICH region is an advantage Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law.

Job-ID32366141Reference26-00829 Job Description: The Immunology and Inflammation group is seeking an independent and highly motivated Temp Sr Associate Scientist to support the intestine and inflammatory disease research.

The Customer Success Associate (Small Business Research Team) fulfills business license research for our high-volume reseller partnerships and our direct clients. Conduct industry and location-specific research for our clients, identifying all federal, state, county, and municipal-level business lic

BEC monitors research outcomes carefully to create effective foundational resources that include strong decoding materials with systematic and explicit instruction and high-quality resources focused on language development and comprehension. BEC is recognized as a responsive publisher that offers eq

Technology and Business consulting services.We are in search of a highly motivated candidate to join our talented team.Job Summary: Our client is seeking a Culture of Innovation Project Manager to drive initiatives that embed innovation mindsets and behaviors across the organization.Reporting to the

Manufacturing-Optical Lab Technician (Sun-Thurs 9pm-6am).The Lab Technician is responsible for the timely, efficient, and accurate processing of products in the lab.Lab Technicians will be assigned an essential function, where he/she will work the predominant portion of their daily work schedule, as

Implements Web solution by monitoring project progress; tracking action items; conducting design and implementation reviews; examining, researching, and resolving issues; escalating issues to appropriate authority; responding to team members' concerns; coordinating requirements with interested depar

Construction Project Manager to join our office team.We are a well-established general contracting and construction management firm specializing in government, commercial, and public-sector construction projects.The ideal candidate must have at least 4 years of similar construction project manageme

Research Assistant Job Duties: Generates hypotheses and designs and performs experiments to test them. Contributes to the preparation of articles on research outcomes and progress and to the submission

A local well respected mechanical contractor is looking for a motivated individual to bring their mechanical experience to a growing dynamic team as an HVAC Project Manager.Ideally, they are looking for someone who enjoys working as a team, has a good attitude and a willingness to work hard.This fas

Data Scientist Job Duties: Formulates and leads guided, multifaceted analytic studies against large volumes of data. Coordinates research and analytic activities utilizing various data points (u

Research, collate, and analyze information to identify key themes and deliver a broad range of standardized training and documentation, advice, or reports to support client projects and programs. Collate and conduct analysis of the tactical and operational information gathered through interviews and

Data Scientist Job Duties: Formulates and leads guided, multifaceted analytic studies against large volumes of data. Coordinates research and analytic activities utilizing various data points (un

Prior experience related to markets, equities research and cryptocurrency trading preferred. Product Owner, Quotes & Research (QNR) - Assistant Vice President. We are seeking a highly motivated product owner to influence, define and execute the digital roadmap for E*TRADE Trading & Investing, with a

The expected salary range for this position is $250,000 - $300,000 depending on experience.NO STAFFING AGENCY CANDIDATES WILL BE CONSIDERED FOR THIS POSITION*.Applicants must be eligible to work in the United States without visa sponsorship now or in the future*.Tutor Perini Company, is seeking

The Senior IT Project Manager is responsible for managing complex IT projects on a day-to-day basis, using the Project Management Life Cycle process and deliverables.Perform project management duties for complex IT projects in accordance with project management life cycle (PMLC) and systems developm

A regionally recognized mechanical construction and facilities services firm is seeking experienced Mechanical Project Managers to support large-scale commercial and industrial projects.This organization provides full lifecycle mechanical solutions including HVAC, plumbing, controls/building automat

Bring your energy to the role of Netflix Data Analyst to adapt to shifting priorities and business needs, work collaboratively across teams and departments, and provide excellent service to customers and team members.Other duties include gain knowledge of company offerings to better serve clients, f

Kimley-Horn has an opportunity for a motivated Senior Project Manager to expand our Land Development practice in White Plains, NY!.The qualified individual will lead a Land Development team while building and managing relationships with key clients.Leadership responsibilities include:.Operating with

Project Manager Manufacturing PMO.At Crestron Electronics, Inc we build the technology that integrates technology.We are proud to be the largest and most recognized brand in automation and control solutions, and the premier technology partner for fortune 500 businesses globally.Our products are int

Our East Water Business is growing and looking for a Construction Project Manager to join their team in New York City, NY! In this role, you will provide project management during the construction phase of our water projects throughout the region (i.The Construction Project Manager directs all phase

This individual will serve a key function in identifying and managing environmental/engineering projects and proposals, conducting engineering research and analysis, and supervising field investigations and laboratory analysis.

Lead and manage the end-to-end migration project of Guidewire PolicyCenter and ClaimCenter from on premise environment to the cloud.Develop and maintain comprehensive project plans, including scope, timelines, milestones, deliverables, and budgets for both systems.Ensure project alignment with organ

Graduate Medical Education (GME) Project Manager.The Graduate Medical Education (GME) Project Manager leads and coordinates institutional GME projects and initiatives that support accreditation, regulatory compliance, educational programming, and operational excellence.Working collaboratively with t

The Assistant Project Manager (APM) will serve as a vital team member while assisting the Senior Project Manager and/or Project Manager on all aspects of a project.APM's will be expected to take on central roles for the oversight of the Project Engineer with a specific focus on document control (RFI

At HDR, our employee-owners are fully engaged in creating a welcoming environment where each of us is valued and respected, a place where everyone is empowered to bring their authentic selves and novel ideas to work every day.We believe transportation is more than movement, it's the foundation of co

Are you looking for a new, exciting opportunity? The time is right to join our Rocky Hill Connecticut PMCM Group and have the opportunity to work on exciting projects throughout the Northeast.Become part of our Team on exciting projects such as Greater Hartford Mobility Program, Task Order Rail, or

Senior Water/Wastewater Project Manager.At HDR, our employee-owners are fully engaged in creating a welcoming environment where each of us is valued and respected, a place where everyone is empowered to bring their authentic selves and novel ideas to work every day.As we work to weave diversity, equ